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Science (New York, N.Y.)
|
May 8, 1992
On the molecular genetics of retinitis pigmentosa
P Humphries, P Kenna, G J Farrar
The Journal of Pediatrics
|
May 1, 1974
Plasma and erythrocyte folate levels in low-birth-weight infants
E D Hibbard, D Obst, A P Kenna
Lancet (London, England)
|
May 16, 1981
Life-threatening illness in those with severe mental handicap
A N Campbel, J R Beasley, A P Kenna
Developmental Medicine and Child Neurology
|
October 1, 1991
Familial infantile myasthenia: a diagnostic problem
J W Matthes, A P Kenna, P R Fawcett
Clinical Genetics
|
July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease
P Humphries, G J Farrar, P Kenna, et al.
The Quarterly Journal of Medicine
|
January 1, 1975
Congenital heart disease in Liverpool: 1960--69
A P Kenna, R W Smithells, D W Fielding
Human Mutation
|
January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions
S A Jordan, G J Farrar, P Kenna, et al.
Human Mutation
|
March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variants
Kevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology
|
May 1, 1995
No evidence of Chlamydia trachomatis infection in children with wheeze
P L Ragunathan, J W Gray, A P Kenna, et al.
Experimental Eye Research
|
April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse
M Campbell, M Humphries, A Kennan, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 80) with videos related to
Sort By:
Page
of 8
Science (New York, N.Y.)
|
May 8, 1992
On the molecular genetics of retinitis pigmentosa
P Humphries, P Kenna, G J Farrar
The Journal of Pediatrics
|
May 1, 1974
Plasma and erythrocyte folate levels in low-birth-weight infants
E D Hibbard, D Obst, A P Kenna
Lancet (London, England)
|
May 16, 1981
Life-threatening illness in those with severe mental handicap
A N Campbel, J R Beasley, A P Kenna
Developmental Medicine and Child Neurology
|
October 1, 1991
Familial infantile myasthenia: a diagnostic problem
J W Matthes, A P Kenna, P R Fawcett
Clinical Genetics
|
July 1, 1990
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease
P Humphries, G J Farrar, P Kenna, et al.
The Quarterly Journal of Medicine
|
January 1, 1975
Congenital heart disease in Liverpool: 1960--69
A P Kenna, R W Smithells, D W Fielding
Human Mutation
|
January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions
S A Jordan, G J Farrar, P Kenna, et al.
Human Mutation
|
March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variants
Kevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology
|
May 1, 1995
No evidence of Chlamydia trachomatis infection in children with wheeze
P L Ragunathan, J W Gray, A P Kenna, et al.
Experimental Eye Research
|
April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse
M Campbell, M Humphries, A Kennan, et al.
Page
of 8